Advanced small cell lung cancer (SCLC): new challenges and new expectations

被引:75
作者
Tsoukalas, Nikolaos [1 ]
Aravantinou-Fatorou, Eleni [2 ]
Baxevanos, Panagiotis [3 ]
Tolia, Maria [4 ]
Tsapakidis, Konstantinos [5 ]
Galanopoulos, Michail [1 ]
Liontos, Michail [6 ]
Kyrgias, George [4 ]
机构
[1] Vet Hosp NIMTS, Dept Oncol, Gennimata N 10-12 Ampelokipi, Athens 11524, Greece
[2] 251 Air Force Hosp, Athens, Greece
[3] Naval Hosp & Vet Med Ctr, Athens, Greece
[4] Univ Thessaly, Sch Hlth Sci, Fac Med, Dept Radiotherapy Radiat Oncol, Larisa, Greece
[5] Univ Thessaly, Sch Hlth Sci, Fac Med, Dept Oncol, Larisa, Greece
[6] Alexandra Gen Hosp, Dept Oncol, Athens, Greece
关键词
Small cell lung cancer (SCLC); biomarkers; immunotherapy; new treatments; new advances; PHASE-II TRIAL; POTENTIAL THERAPEUTIC TARGET; IN-VIVO; SURGICAL SPECIMENS; DOUBLE-BLIND; STAGE; CHEMOTHERAPY; INHIBITOR; BEVACIZUMAB; CARCINOMA;
D O I
10.21037/atm.2018.03.31
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Small cell lung cancer (SCLC) remains one of the most lethal malignancies and a major health riddle. The therapeutic options are limited. The combination of etoposide or irinotecan with platinum chemotherapy is the standard of care at any stage. The last decade systemic efforts have been done to reveal specific therapeutic targets for small cell lung carcinomas. In this review, we focus on the new therapeutic strategies of SCLC, including immune-related treatment that may change the prognosis of the disease. The main genetic mutations observed in SCLC are TP53 and RB1 mutations; however, it is well known that these molecules are not yet targetable. In recent years, research has revealed other frequent genetic alterations and activated signaling pathways that might be an effective treatment target. Loss of PTEN, activating PI3K mutations, inhibition of NOTCH pathway and aurora kinase activation are among them. Moreover, FDGFR1 amplification, activation of the Hedgehog pathway and repair-protein PARP1 seem to participate in SCLC tumorigenesis. These new findings have identified some interesting targets. Moreover, immunotherapy tries to find its place in the treatment of SCLC. Immune checkpoint inhibitors are under investigation in phase I to III clinical trials. We hope that in next years the treatment of SCLC patients will be improved with the administration of targeting therapy and the introduction of immunotherapy.
引用
收藏
页数:8
相关论文
共 60 条
[1]   Southwest Oncology Group S0802: A Randomized, Phase II Trial of Weekly Topotecan With and Without Ziv-Aflibercept in Patients With Platinum-Treated Small-Cell Lung Cancer [J].
Allen, Jeffrey W. ;
Moon, James ;
Redman, Mary ;
Gadgeel, Shirish M. ;
Kelly, Karen ;
Mack, Philip C. ;
Saba, Hanna M. ;
Mohamed, Mohamed K. ;
Jahanzeb, Mohammad ;
Gandara, David R. .
JOURNAL OF CLINICAL ONCOLOGY, 2014, 32 (23) :2463-2470
[2]   Targeted therapies for small cell lung cancer: Where do we stand? [J].
Arcaro, Alexandre .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2015, 95 (02) :154-164
[3]  
Belani CP, 2013, J CLIN ONCOL S, V31, P7508, DOI DOI 10.1200/JCO.2013.31.15_SUPPL.7508
[4]   Proteomic Profiling Identifies Dysregulated Pathways in Small Cell Lung Cancer and Novel Therapeutic Targets Including PARP1 [J].
Byers, Lauren Averett ;
Wang, Jing ;
Nilsson, Monique B. ;
Fujimoto, Junya ;
Saintigny, Pierre ;
Yordy, John ;
Giri, Uma ;
Peyton, Michael ;
Fan, You Hong ;
Diao, Lixia ;
Masrorpour, Fatemeh ;
Shen, Li ;
Liu, Wenbin ;
Duchemann, Boris ;
Tumula, Praveen ;
Bhardwaj, Vikas ;
Welsh, James ;
Weber, Stephanie ;
Glisson, Bonnie S. ;
Kalhor, Neda ;
Wistuba, Ignacio I. ;
Girard, Luc ;
Lippman, Scott M. ;
Mills, Gordon B. ;
Coombes, Kevin R. ;
Weinstein, John N. ;
Minna, John D. ;
Heymach, John V. .
CANCER DISCOVERY, 2012, 2 (09) :798-811
[5]   Proteomic Markers of DNA Repair and PI3K Pathway Activation Predict Response to the PARP Inhibitor BMN 673 in Small Cell Lung Cancer [J].
Cardnell, Robert J. ;
Feng, Ying ;
Diao, Lixia ;
Fan, You-Hong ;
Masrorpour, Fatemah ;
Wang, Jing ;
Shen, Yuqiao ;
Mills, Gordon B. ;
Minna, John D. ;
Heymach, John V. ;
Byers, Lauren A. .
CLINICAL CANCER RESEARCH, 2013, 19 (22) :6322-6328
[6]   Notch inhibition by the ligand Delta-Like 3 defines the mechanism of abnormal vertebral segmentation in spondylocostal dysostosis [J].
Chapman, Gavin ;
Sparrow, Duncan B. ;
Kremmer, Elisabeth ;
Dunwoodie, Sally L. .
HUMAN MOLECULAR GENETICS, 2011, 20 (05) :905-916
[7]   Targeting Transcriptional Addictions in Small Cell Lung Cancer with a Covalent CDK7 Inhibitor [J].
Christensen, Camilla L. ;
Kwiatkowski, Nicholas ;
Abraham, Brian J. ;
Carretero, Julian ;
Al-Shahrour, Fatima ;
Zhang, Tinghu ;
Chipumuro, Edmond ;
Herter-Sprie, Grit S. ;
Akbay, Esra A. ;
Altabef, Abigail ;
Zhang, Jianming ;
Shimamura, Takeshi ;
Capelletti, Marzia ;
Reibel, Jakob B. ;
Cavanaugh, Jillian D. ;
Gao, Peng ;
Liu, Yan ;
Michaelsen, Signe R. ;
Poulsen, Hans S. ;
Aref, Amir R. ;
Barbie, David A. ;
Bradner, James E. ;
George, Rani E. ;
Gray, Nathanael S. ;
Young, Richard A. ;
Won, Kwok-Kin .
CANCER CELL, 2014, 26 (06) :909-922
[8]   A Phase II Study of the Histone Deacetylase Inhibitor Panobinostat (LBH589) in Pretreated Patients with Small-Cell Lung Cancer [J].
de Marinis, Filippo ;
Atmaca, Akin ;
Tiseo, Marcello ;
Giuffreda, Libero ;
Rossi, Antonio ;
Gebbia, Vittorio ;
D'Antonio, Chiara ;
Dal Zotto, Laura ;
Al-Batran, Salah-Eddin ;
Marsoni, Silvia ;
Wolf, Martin .
JOURNAL OF THORACIC ONCOLOGY, 2013, 8 (08) :1091-1094
[9]   In vivo efficacy of STI571 in xenografted human small cell lung cancer alone or combined with chemotherapy [J].
Decaudin, D ;
de Cremoux, P ;
Sastre, X ;
Judde, JG ;
Nemati, F ;
Tran-Perennou, C ;
Fréneaux, P ;
Livartowski, A ;
Pouillart, P ;
Poupon, MF .
INTERNATIONAL JOURNAL OF CANCER, 2005, 113 (05) :849-856
[10]   Notch inhibitors for cancer treatment [J].
Espinoza, Ingrid ;
Miele, Lucio .
PHARMACOLOGY & THERAPEUTICS, 2013, 139 (02) :95-110